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FDA 510(k)

A-PORT IMPLANT VASCULAR ACCESS SYST CATH - 75CM

K-Number: K921475 · 1992-10-16

ApplicantTherex Corp.
Decision Date1992-10-16
Product CodeLJT
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

A-PORT IMPLANT VASCULAR ACCESS SYST CATH - 75CM is the device name listed in this FDA 510(k) record. The listed applicant is Therex Corp.. It received FDA 510(k) clearance on 1992-10-16 under 510(k) number K921475. The device is classified under product code LJT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the A-PORT IMPLANT VASCULAR ACCESS SYST CATH - 75CM?

A-PORT IMPLANT VASCULAR ACCESS SYST CATH - 75CM is a medical device that received FDA 510(k) clearance on 1992-10-16. The listed applicant is Therex Corp.. The 510(k) number is K921475.

When did A-PORT IMPLANT VASCULAR ACCESS SYST CATH - 75CM receive FDA 510(k) clearance?

A-PORT IMPLANT VASCULAR ACCESS SYST CATH - 75CM received FDA 510(k) clearance on 1992-10-16, under 510(k) number K921475.

Who is the listed applicant for A-PORT IMPLANT VASCULAR ACCESS SYST CATH - 75CM?

The FDA 510(k) record lists Therex Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for A-PORT IMPLANT VASCULAR ACCESS SYST CATH - 75CM?

The FDA product code for A-PORT IMPLANT VASCULAR ACCESS SYST CATH - 75CM is LJT.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Therex Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: LJT)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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